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Fixation or non-fixation of mesh in laparoscopic inguinal hernia repair

Not Applicable
Conditions
Inguinal hernia.
Inguinal hernia
Registration Number
IRCT20190204042618N4
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
86
Inclusion Criteria

No history of hernia repair surgery
No history of laparotomy
No strangulated or incarcerated hernia
Were satisfied to participate in the study

Exclusion Criteria

Cancellation of the surgery for any reason
Occurrence of unwanted complications during the surgery resulting in serious complications or death
Non-referral of the patient in post-operative follow-up for any reasons
Dissatisfaction to continue the collaboration in the present study

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of pain. Timepoint: One day after surgery, when releasing the hospital, one and two weeks and one and 6 months after surgery. Method of measurement: VAS (Visual analogue scale).;Early and late complications. Timepoint: The first week after surgery and in two weeks, one month, and six months after surgery. Method of measurement: Periodic Regular Examination.;Hernia relapse. Timepoint: The first week after surgery and in two weeks, one month, and six months after surgery. Method of measurement: Periodic Regular Examination.
Secondary Outcome Measures
NameTimeMethod
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